Recall due to an increased number of adverse event reports

Recall due to reduced release of active pharmaceutical ingredient

Recall due to reduced release of active pharmaceutical ingredient

Recall due to visible particles

Recall due to not registered serial numbers

Recall due to nitrosamine contamination above the permitted daily dose

Recall due to incorrect labelling

Recall due to deactivated serial numbers

Recall due to the possibility of powder clumping in the capsule

Recall due to incorrect labelling of active substance content